01 1CKD Bio Corporation
02 1CSPC Shengxue Glucose Co. , Ltd.
03 1Zhejiang Hisun Pharmaceutical Co. , Ltd.
01 3Acarbose
01 2China
02 1South Korea
Registration Number : 220MF10038
Registrant's Address : 8, Chungjeong-ro, Seodaemun-gu, Seoul, Republic of Korea
Initial Date of Registration : 2008-02-05
Latest Date of Registration : 2008-02-05
Registration Number : 303MF10047
Registrant's Address : No. 48 Shengxue Road, Luncheng District, Shijiazhuang City, Hebei Province, China
Initial Date of Registration : 2021-03-17
Latest Date of Registration : 2021-03-17
Registration Number : 218MF10411
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 3180...
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2007-01-17
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PharmaCompass offers a list of Acarbose API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Acarbose manufacturer or Acarbose supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acarbose manufacturer or Acarbose supplier.
PharmaCompass also assists you with knowing the Acarbose API Price utilized in the formulation of products. Acarbose API Price is not always fixed or binding as the Acarbose Price is obtained through a variety of data sources. The Acarbose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC, including repackagers and relabelers. The FDA regulates HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC supplier is an individual or a company that provides HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC active pharmaceutical ingredient (API) or HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC finished formulations upon request. The HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC suppliers may include HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC API manufacturers, exporters, distributors and traders.
click here to find a list of HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC Drug Master File in Japan (HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC JDMF) empowers HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC JDMF during the approval evaluation for pharmaceutical products. At the time of HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC suppliers with JDMF on PharmaCompass.
We have 3 companies offering HMC-(1-4)AGL-(1-4)GLC-(1-4)GLC
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